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Hydrochloric Acid → 5-(N-formyl-N-methylamino-methyl)isatoic anhydride

HRID 557454
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HRID 557454 반응식
[C:1](N1C=CN=C1)(N1C=CN=C1)=[O:2].[NH2:13][C:14]1[CH:22]=[CH:21][C:20]([CH2:23][N:24]([CH:26]=[O:27])[CH3:25])=[CH:19][C:15]=1[C:16]([OH:18])=[O:17].Cl>CN(C)C=O>[CH:26]([N:24]([CH2:23][C:20]1[CH:19]=[C:15]2[C:16]([O:18][C:1](=[O:2])[NH:13][C:14]2=[CH:22][CH:21]=1)=[O:17])[CH3:25])=[O:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 682631,1'-CarbonyldiimidazoleHCID 580183122-amino-5-(N-formyl-N-methylamino-methyl)benzoic acid

생성물 1

HCID 251343765-(N-formyl-N-methylamino-methyl)isatoic anhydride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

There was suspended, in 15.2 mL of N,N-dimethylformamide, 3.82 g of 1,1′-carbonyl-diimidazole (CDI) and the resulting suspension was cooled to 5° C. To this slurry, there was added 4.0 g of 2-amino-5-(N-formyl-N-methylamino-methyl)benzoic acid in two portions, followed by the stirring of the same for one hour. After the confirmation of the disappearance of the starting material by HPLC, seed crystals were added to the slurry while dropwise adding 40.3 mL of a 1M hydrochloric acid aqueous solution to separate out solid and the resulting solid was isolated through filtration under reduced pressure. After washing the solid with 120 mL of water, it was dried at 70° C. for 13 hours under reduced pressure to thus give 3.20 g of the title compound as a white solid.

후처리

  1. additionAfter the confirmation of the disappearance of the starting material by HPLC, seed crystals were added to the slurry
  2. customto separate out solid
  3. customthe resulting solid was isolated through filtration under reduced pressure
  4. washAfter washing the solid with 120 mL of water, it
  5. dry with materialwas dried at 70° C. for 13 hours under reduced pressure to thus give 3.20 g of the title compound as a white solid

출처 및 근거

ORD 기록
ord-a21db31cc10842c1bee1ef073c323839
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08058432B2

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